Evidence map›Paper›PMID 33385878›Full record

ReviewMedical hypotheses2021

The plausible mechanisms of tramadol for treatment of COVID-19.

Nahla E El-Ashmawy, Abdel-Halim A Lashin, Kamal M Okasha, Amal M Abo Kamer, Tarek M Mostafa, Mona El-Aasr, Ahmed E Goda, Yusuf A Haggag, Haytham O Tawfik, Mariam A Abo-Saif

Open access · greenAbstract readReview
In one paragraph

Review in Medical hypotheses, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.4field-weighted citation impact, top 26% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 1 institution in 1 country.

Nahla E El-AshmawyBiochemistry Department, Faculty of Pharmacy, Tanta University, Tanta, Egypt.
Abdel-Halim A LashinMedicinal Chemistry Department, Faculty of Pharmacy, Tanta University, Tanta, Egypt.
Kamal M OkashaInternal Medicine and Nephrology Department, Faculty of Medicine, Tanta University, Tanta, Egypt.
Amal M Abo KamerMicrobiology Department, Faculty of Pharmacy, Tanta University, Tanta, Egypt.
Tarek M MostafaClinical Pharmacy Department, Faculty of Pharmacy, Tanta University, Tanta, Egypt.
Mona El-AasrPharmacognosy Department, Faculty of Pharmacy, Tanta University, Tanta, Egypt.
Ahmed E GodaPharmacology Department, Faculty of Pharmacy, Tanta University, Tanta, Egypt.
Yusuf A HaggagPharmaceutical Technology Department, Faculty of Pharmacy, Tanta University, Tanta, Egypt.
Haytham O TawfikMedicinal Chemistry Department, Faculty of Pharmacy, Tanta University, Tanta, Egypt.
Mariam A Abo-SaifBiochemistry Department, Faculty of Pharmacy, Tanta University, Tanta, Egypt. Electronic address: maryem_abosaif@pharm.tanta.edu.eg.
Tanta University · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Currently, no single medication has been approved for the management of coronavirus disease-2019 (COVID-19) caused by the new severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Therefore, drug repositioningby investigating the use of existing drugs for management of COVID-19 patients is considered a desperate need. Tramadol is a commonly prescribed analgesic drug for treatment of moderate to severe pain with less potential for dependence and respiratory depression. Multiple evidence support that tramadol is a promising drug for treatment of COVID-19 patients. Herein, we discuss the possible beneficial effects of using tramadol against SARS-CoV-2 infection and their underlying mechanism of action. The anti-inflammatory effect of tramadol may help to suppress the COVID-19 related cytokine storm through decreasing interleukin (IL)-6, tumor necrosis factor-alpha (TNF-α), and C-reactive protein (CRP). Besides, tramadol activates natural killer (NK) and T-cells and enhances IL-2 secretion, which produce immune-enhancing effect against SARS-CoV-2. Recent studies confirmed that COVID-19 patients with acute respiratory failure showed increased fibrin formation and polymerization that may lead to thrombosis. Tramadol owing to its hypocoagulable effect may protect against venous thromboembolism in these patients. Moreover, tramadol can exert a cardioprotective effect via decreasing lactate dehydrogenase (LDH) level which is elevated in most of patients with COVID-19. Furthermore, the severity and mortality of COVID-19 have been correlated with old age patients, which may be due to the lack of antioxidant mechanisms and increased oxidative damage. Tramadol could protect COVID-19 patient from disease complications by increases the antioxidant enzymes superoxide dismutase and glutathione peroxidase while diminished malondialdehyde. More interestingly, tramadol as an effective analgesic and antitussive may have a beneficial effect on COVID-19 patients suffering from cough, headache, ache, and pain. The tramadol anti-psychotic effect may also protect against psychiatric disorders associated with SARS-CoV-2 infection. Moreover, tramadol has bactericidal activity against a wide range of pathogens including Pseudomonas aeruginosa which is common in severe COVID-19 patients leading to pneumonia with worse clinical outcomes. Therefore, we hypothesize that tramadol might be a promising adjuvant therapeutic option against SARS-CoV-2 infection. Based on that, tramadol should be considered as adjuvant therapy for COVID-19 clinical trials.

Indexed as

COVID-19 Drug TreatmentAnalgesics, OpioidAnti-Bacterial AgentsAntidepressive AgentsAnti-Inflammatory AgentsAntioxidantsCOVID-19Drug RepositioningHumansImmunologic FactorsModels, BiologicalPandemicsSARS-CoV-2TramadolAnalgesics, OpioidAnti-Bacterial AgentsAntidepressive AgentsAnti-Inflammatory AgentsAntioxidantsImmunologic FactorsTramadolAnti-inflammatoryCOVID-19Hypocoagulable effectImmune-enhancingSARS-CoV-2Tramadol

Identifiers

PMID33385878
PMCPMC7831961
OpenAlexW3114798172

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.